Canonical Allele Identifier: PA2580176620
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1730284
ClinVar RCV Id: RCV002326460
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230673.1:p.Asn111Ser
CA5137778
NM_001243744.2:c.332A>G